celecoxib
Generic: celecoxib
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
celecoxib
Generic Name
celecoxib
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
celecoxib 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3292
Product ID
70518-3292_3a710d7d-cf26-48ae-e063-6394a90a5142
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210628
Listing Expiration
2026-12-31
Marketing Start
2021-12-13
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183292
Hyphenated Format
70518-3292
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
celecoxib (source: ndc)
Generic Name
celecoxib (source: ndc)
Application Number
ANDA210628 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 45 CAPSULE in 1 BOTTLE, PLASTIC (70518-3292-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a710d7d-cf26-48ae-e063-6394a90a5142", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["JCX84Q7J1L"], "rxcui": ["205323"], "spl_set_id": ["8c4b224e-7227-426c-98f3-33b9b7324e84"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "45 CAPSULE in 1 BOTTLE, PLASTIC (70518-3292-3)", "package_ndc": "70518-3292-3", "marketing_start_date": "20250305"}], "brand_name": "CELECOXIB", "product_id": "70518-3292_3a710d7d-cf26-48ae-e063-6394a90a5142", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-3292", "generic_name": "CELECOXIB", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CELECOXIB", "active_ingredients": [{"name": "CELECOXIB", "strength": "200 mg/1"}], "application_number": "ANDA210628", "marketing_category": "ANDA", "marketing_start_date": "20211213", "listing_expiration_date": "20261231"}